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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H25ClN2O4S
Molecular Weight 448.963
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLENTIAZEM

SMILES

COC1=CC=C(C=C1)[C@@H]2SC3=CC(Cl)=CC=C3N(CCN(C)C)C(=O)[C@@H]2OC(C)=O

InChI

InChIKey=GYKFWCDBQAFCLJ-RTWAWAEBSA-N
InChI=1S/C22H25ClN2O4S/c1-14(26)29-20-21(15-5-8-17(28-4)9-6-15)30-19-13-16(23)7-10-18(19)25(22(20)27)12-11-24(2)3/h5-10,13,20-21H,11-12H2,1-4H3/t20-,21+/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H25ClN2O4S
Molecular Weight 448.963
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Clentiazem is a chloride derivative of diltiazem, originated in Tanabe Seiyaku. It works as a blocker of calcium channels. The drug was investigated in the clinical trials for the treatment of stable angina, and essential hypertension. Despite the positive results of clinical trials, no development of the drug was reported.

Approval Year

PubMed

PubMed

TitleDatePubMed
1,5-Benzothiazepine, a versatile pharmacophore: a review.
2008-11
Effects of first and second generation calcium channel blockers on diastolic function of the failing hamster heart: relationship with coronary flow changes.
2003-07
Sex-related differences in the renal disposition of the acidic metabolite of clentiazem in rat.
2001-10
Protective effect of clentiazem against epinephrine-induced cardiac injury in rats.
1993-07
Protective effects of the calcium antagonists diltiazem and TA3090 against hepatic injury due to hypoxia.
1992-12-01
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:22:27 GMT 2025
Edited
by admin
on Mon Mar 31 18:22:27 GMT 2025
Record UNII
40DK034DRC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLENTIAZEM
INN   MI   WHO-DD  
INN  
Official Name English
CLENTIAZEM [MI]
Preferred Name English
clentiazem [INN]
Common Name English
Clentiazem [WHO-DD]
Common Name English
(+)-(2S,3S)-8-CHLORO-5-(2-(DIMETHYLAMINO)ETHYL)-2,3-DIHYDRO-3-HYDROXY-2-(P-METHOXYPHENYL)-1,5-BENZOTHIAZEPIN-4(5H)-ONE ACETATE (ESTER)
Common Name English
1,5-BENZOTHIAZEPIN-4(5H)-ONE, 3-(ACETYLOXY)-8-CHLORO-5-(2-(DIMETHYLAMINO)ETHYL)-2,3-DIHYDRO-2-(4-METHOXYPHENYL)-, (2S-CIS)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
Code System Code Type Description
CAS
96125-53-0
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
WIKIPEDIA
CLENTIAZEM
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
EVMPD
SUB06653MIG
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
SMS_ID
100000080214
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
ChEMBL
CHEMBL165667
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID901028074
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
FDA UNII
40DK034DRC
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
MERCK INDEX
m3616
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY Merck Index
INN
6453
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
MESH
C056595
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
NCI_THESAURUS
C81679
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
PUBCHEM
57026
Created by admin on Mon Mar 31 18:22:27 GMT 2025 , Edited by admin on Mon Mar 31 18:22:27 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY